doxycycline hyclate

Generic: doxycycline hyclate

Labeler: health department, oklahoma state
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler health department, oklahoma state
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

doxycycline hyclate 100 mg/1

Manufacturer
Health Department, Oklahoma State

Identifiers & Regulatory

Product NDC 83112-100
Product ID 83112-100_47479ed6-5616-c375-e063-6294a90afef4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062269
Listing Expiration 2027-12-31
Marketing Start 2025-03-07

Pharmacologic Class

Classes
tetracycline-class drug [epc] tetracyclines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83112100
Hyphenated Format 83112-100

Supplemental Identifiers

RxCUI
1649988 1650143
UNII
19XTS3T51U

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name doxycycline hyclate (source: ndc)
Generic Name doxycycline hyclate (source: ndc)
Application Number ANDA062269 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 14 TABLET, FILM COATED in 1 PACKET (83112-100-00)
  • 14 TABLET, FILM COATED in 1 PACKET (83112-100-14)
  • 20 TABLET, FILM COATED in 1 PACKET (83112-100-20)
  • 28 TABLET, FILM COATED in 1 PACKET (83112-100-28)
  • 42 TABLET, FILM COATED in 1 PACKET (83112-100-42)
  • 56 TABLET, FILM COATED in 1 PACKET (83112-100-56)
source: ndc

Packages (6)

Ingredients (1)

doxycycline hyclate (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47479ed6-5616-c375-e063-6294a90afef4", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1649988", "1650143"], "spl_set_id": ["f39365f9-eb64-00cb-e053-2995a90a8d80"], "manufacturer_name": ["Health Department, Oklahoma State"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 PACKET (83112-100-00)", "package_ndc": "83112-100-00", "marketing_start_date": "20250307"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 PACKET (83112-100-14)", "package_ndc": "83112-100-14", "marketing_start_date": "20250307"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 PACKET (83112-100-20)", "package_ndc": "83112-100-20", "marketing_start_date": "20250307"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 PACKET (83112-100-28)", "package_ndc": "83112-100-28", "marketing_start_date": "20250307"}, {"sample": false, "description": "42 TABLET, FILM COATED in 1 PACKET (83112-100-42)", "package_ndc": "83112-100-42", "marketing_start_date": "20250307"}, {"sample": false, "description": "56 TABLET, FILM COATED in 1 PACKET (83112-100-56)", "package_ndc": "83112-100-56", "marketing_start_date": "20250307"}], "brand_name": "Doxycycline Hyclate", "product_id": "83112-100_47479ed6-5616-c375-e063-6294a90afef4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "83112-100", "generic_name": "Doxycycline Hyclate", "labeler_name": "Health Department, Oklahoma State", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA062269", "marketing_category": "ANDA", "marketing_start_date": "20250307", "listing_expiration_date": "20271231"}